Study register · detail
No direction reported
1860 citations
SampleLeitlinie
Durationunclear
EndpointPharmacological therapy…
Blindingn.a.
DesignLeitlinie (EFNS Task Force)
Key finding
Guideline on the evidence assessment of pharmacological treatments for neuropathic pain; several medications (TCA, pregabalin, gabapentin, tramadol, opioids, duloxetine, venlafaxine, topical lidocaine, capsaicin patch) show Level A evidence in various indications.
Summary
EFNS guideline 2010 on the pharmacological treatment of neuropathic pain; Level A evidence for tricyclic antidepressants, pregabalin, gabapentin, tramadol and opioids (for various etiologies including diabetic polyneuropathy, post-herpetic neuralgia). Combination therapy TCA-gabapentin and gabapentin-opioids Level A.
P
PopulationAdults with neuropathic pain of various etiologies (esp. diabetic polyneuropathy, postherpetic neuralgia, among others)
I
InterventionPharmacological therapy: TCA, pregabalin, gabapentin, tramadol, opioids, duloxetine, venlafaxine, topical lidocaine, capsaicin patch, combination therapies
O
OutcomeLevel A evidence for TCA, pregabalin, gabapentin, tramadol, opioids (various indications), duloxetine, venlafaxine, topical lidocaine and capsaicin patch (restricted indications); combination therapy TCA-gabapentin and gabapentin-opioids also Level A
Quality profile
Sample size
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Blinding
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Effect size
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Citations / year
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Abstract
Background And Objectives: This second European Federation of Neurological Societies Task Force aimed at updating the existing evidence about the pharmacological treatment of neuropathic pain since 2005.
Methods: Studies were identified using the Cochrane Database and Medline. Trials were classified according to the aetiological condition. All class I and II randomized controlled trials (RCTs) were assessed; lower class studies were considered only in conditions that had no top-level studies. Treatments administered using repeated or single administrations were considered, provided they are feasible in an outpatient setting.
Results: Most large RCTs included patients with diabetic polyneuropathies and post-herpetic neuralgia, while an increasing number of smaller studies explored other conditions. Drugs generally have similar efficacy in various conditions, except in trigeminal neuralgia, chronic radiculopathy and HIV neuropathy, with level A evidence in support of tricyclic antidepressants (TCA), pregabalin, gabapentin, tramadol and opioids (in various conditions), duloxetine, venlafaxine, topical lidocaine and capsaicin patches (in restricted conditions). Combination therapy appears useful for TCA-gabapentin and gabapentin-opioids (level A).
Conclusions: There are still too few large-scale comparative studies. For future trials, we recommend to assess comorbidities, quality of life, symptoms and signs with standardized tools and attempt to better define responder profiles to specific drug treatments.
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